Canonical Allele Identifier: CA657458980

Gene: KLK3

Linked Data

• COSMIC: COSN21444665

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860246_50860247insC , CM000681.2:g.50860246_50860247insC	GRCh38
NC_000019.9:g.51363502_51363503insC , CM000681.1:g.51363502_51363503insC	GRCh37
NC_000019.8:g.56055314_56055315insC	NCBI36
NG_011653.1:g.10332_10333insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.*119_*120insC MANE Select	ENSP00000314151.1:n.*119_*120insC
ENST00000326003.6:c.*119_*120insC	ENSP00000314151.1:n.*119_*120insC
ENST00000360617.7:c.1347_1348insC	ENSP00000353829.2:n.1347_1348insC
ENST00000422986.6:c.*561_*562insC	ENSP00000393628.2:n.*561_*562insC
ENST00000595392.5:c.*406_*407insC	ENSP00000468912.1:n.*406_*407insC
ENST00000595952.5:c.*119_*120insC	ENSP00000471155.1:n.*119_*120insC
ENST00000596333.1:n.1083_1084insC
ENST00000601349.5:n.2184_2185insC
ENST00000617027.4:c.*119_*120insC	ENSP00000483513.1:n.*119_*120insC
NM_001030047.1:c.*630_*631insC	NP_001025218.1:n.*630_*631insC
NM_001030048.1:c.*119_*120insC	NP_001025219.1:n.*119_*120insC
NM_001648.2:c.*119_*120insC MANE Select	NP_001639.1:n.*119_*120insC
XM_011526923.1:c.*119_*120insC	XP_011525225.1:n.*119_*120insC
XR_935817.1:n.1324+992_1324+993insC